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Nanofibres in drug delivery /

In recent years there has been an explosion of interest in the production of nanoscale fibres for drug delivery and tissue engineering. Nanofibres in Drug Delivery aims to outline to new researchers in the field the utility of nanofibres in drug delivery, and to explain to them how to prepare fibres...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Autores principales: Williams, Gareth R. (Autor), Raimi-Abraham, Bahijja T. (Autor), Luo, C. J. (Autor)
Formato: Electrónico eBook
Idioma:Inglés
Publicado: London : UCL Press, 2018.
Temas:
Acceso en línea:Texto completo

MARC

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100 1 |a Williams, Gareth R.,  |e author. 
245 1 0 |a Nanofibres in drug delivery /  |c Gareth R. Williams, Bahijja T. Raimi-Abraham, C.J. Luo. 
264 1 |a London :  |b UCL Press,  |c 2018. 
300 |a 1 online resource :  |b illustrations (some color) 
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504 |a Includes bibliographical references. 
588 0 |a Print version record. 
520 |a In recent years there has been an explosion of interest in the production of nanoscale fibres for drug delivery and tissue engineering. Nanofibres in Drug Delivery aims to outline to new researchers in the field the utility of nanofibres in drug delivery, and to explain to them how to prepare fibres in the laboratory. The book begins with a brief discussion of the main concepts in pharmaceutical science. The authors then introduce the key techniques that can be used for fibre production and explain briefly the theory behind them. They discuss the experimental implementation of fibre production, starting with the simplest possible set-up and then moving on to consider more complex arrangements. As they do so, they offer advice from their own experience of fibre production, and use examples from current literature to show how each particular type of fibre can be applied to drug delivery. They also consider how fibre production could be moved beyond the research laboratory into industry, discussing regulatory and scale-up aspects. 
546 |a English. 
505 0 |a Intro; Half Title; Title Page; Copyright Page; Acknowledgements; Contents; List of figures; List of abbreviations; 1 Introduction; 1.1 Preamble; 1.2 Nanofibres; 1.3 Key concepts in drug delivery; 1.3.1 The therapeutic window and bioavailability; 1.3.2 Modified-release systems; 1.3.3 Dissolution, solubility and permeability; 1.3.4 Physical form; 1.4 Nanofibre characterisation; 1.4.1 Electron microscopy; 1.4.2 X-ray diffraction; 1.4.3 Thermal methods; 1.4.4 Infrared spectroscopy; 1.4.5 Functional performance; 1.4.5.1 Dissolution and permeability testing; 1.4.5.2 API quantification 
505 8 |a 1.4.6 Stability studies1.5 An overview of contemporary pharmaceutical technology; 1.5.1 Hot melt extrusion; 1.5.2 Spray drying; 1.5.3 Freeze drying; 1.5.4 Nanofibre manufacturing; 1.6 Summary; References; 2 Electrospinning fundamentals; 2.1 Background; 2.2 A brief history of electrospinning; 2.3 EHD fundamentals; 2.4 Understanding the electrospinning process; 2.4.1 Jet initiation; 2.4.2 Electrospinning vs. electrospraying; 2.4.3 Jet elongation: bending and whipping; 2.4.4 Jet solidification; 2.5 The parameters affecting electrospinning; 2.5.1 Solution parameters; 2.5.2 Processing parameters 
505 8 |a 2.5.3 Environmental parameters2.5.4 Solvent and polymer selection; 2.6 The experimental set-up; 2.6.1 Basics; 2.6.2 The power supply and syringe pump; 2.6.3 The spinneret; 2.6.4 The collector; 2.6.5 Other considerations; 2.6.6 Establishing and troubleshooting an electrospinning process; 2.7 Fibre properties; 2.8 Characterisation; 2.9 Summary; References; 3 Monoaxial electrospinning; 3.1 Introduction; 3.2 Experimental considerations; 3.2.1 Solution parameters; 3.2.2 Processing parameters; 3.2.3 The spinneret; 3.2.4 Polymer choice; 3.2.5 Starting experimental work; 3.3 Fibre properties 
505 8 |a 3.4 Some typical results3.5 Fast-dissolving drug delivery systems; 3.5.1 Electrospun fast-dissolving drug delivery systems; 3.5.2 Caveats; 3.5.3 Multicomponent formulations; 3.5.4 Stability; 3.6 Extended-release systems; 3.6.1 Applications; 3.6.2 Drawbacks and release mechanisms; 3.7 pH-controlled delivery; 3.7.1 Oral administration; 3.7.2 Anticancer applications; 3.8 Pulsatile release; 3.9 Multilayer materials; 3.10 Thermoresponsive systems; 3.11 Emulsion and suspension electrospinning; 3.11.1 Emulsions; 3.11.2 Suspensions; 3.12 Tissue-engineering applications 
505 8 |a 3.13 Using fibres as sacrificial templates3.14 Conclusions; References; 4 Coaxial and multi-axial electrospinning; 4.1 Introduction; 4.2 Experimental considerations; 4.2.1 Handling two liquids; 4.2.2 The spinneret and electrodes; 4.2.3 Establishing a coaxial process; 4.3 Extended-release systems; 4.3.1 Preventing burst release; 4.3.2 Biphasic release; 4.4 Targeted drug delivery; 4.5 Multifunctional materials; 4.6 Other applications; 4.7 Protein delivery systems; 4.8 Cell electrospinning; 4.9 Modified coaxial spinning; 4.10 Triaxial and quad-axial systems; 4.11 Conclusions; References 
590 |a JSTOR  |b Books at JSTOR Open Access 
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650 0 |a Drug delivery devices. 
650 0 |a Nanofibers. 
650 1 2 |a Drug Delivery Systems 
650 1 2 |a Nanofibers 
650 6 |a Médicaments  |x Administration  |x Dispositifs. 
650 6 |a Nanofibres. 
650 7 |a nanofiber.  |2 aat 
650 7 |a Pharmaceutical industries.  |2 bicssc 
650 7 |a Other branches of medicine.  |2 bicssc 
650 7 |a Therapy & therapeutics.  |2 bicssc 
650 7 |a Business & Economics  |x Industries  |x Pharmaceutical & Biotechnology.  |2 bisacsh 
650 7 |a Medical  |x Military Medicine.  |2 bisacsh 
650 7 |a Medical.  |2 bisacsh 
650 7 |a Drug delivery devices  |2 fast 
650 7 |a Nanofibers  |2 fast 
653 |a Nanofibres. 
653 |a Drugs. 
653 |a Drug delivery. 
700 1 |a Raimi-Abraham, Bahijja T.,  |e author. 
700 1 |a Luo, C. J.,  |e author. 
776 0 8 |i Print version:  |a WILLIAMS, GARETH R. RAIMI-ABRAHAM, BAHIJJA T. LUO, C.J.  |t NANOFIBRES IN DRUG DELIVERY.  |d [Place of publication not identified] : UCL PRESS, 2018  |z 1787350231  |w (OCoLC)1036771631 
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